A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986822



Internal ID58654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88621020..88621123hg38UCSC Ensembl
chr6:89330739..89330842hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454323
Supporting Variants
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986822
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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